Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
HLA-haploidentical donor lymphocyte infusion (DLI) is an investigational cellular immunotherapy developed by Duke University for the treatment of high-risk acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS), particularly in older patients. Evaluated in clinical trials such as NCT02046122, this therapy involves the adoptive transfer of CD3+ T-lymphocytes obtained from partially matched (HLA-haploidentical) family donors. The treatment is designed to induce a graft-versus-leukemia (GVL) effect, where the donor's immune cells recognize and eliminate residual malignant cells in the recipient. In the Duke University protocol, this infusion is administered following a chemotherapy conditioning regimen (typically idarubicin and cytarabine) to maximize efficacy and reduce the risk of graft-versus-host disease (GVHD). This approach aims to provide a viable and less toxic alternative to standard allogeneic hematopoietic stem cell transplantation for elderly patients who are not candidates for intensive transplant procedures.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on HLA-haploidentical donor lymphocyte infusion.